The following articles (labelled with PubMed ID or TBD) are for your review
| PMID | Data | Article Title | Organization |
|---|
| 7515442 |
9 |
14 alpha,14' beta-[Dithiobis[(2-oxo-2,1-ethanediyl)imino]]bis (7,8-dihydromorphinone) and 14 alpha,14' beta-[dithiobis[(2-oxo-2,1- ethanediyl)imino]]bis[7,8-dihydro-N-(cyclopropylmethyl)normorphinone]: chemistry and opioid binding properties. |
Institute |
| 2165166 |
13 |
Electrophilic alpha-methylene-gamma-lactone and isothiocyanate opioid ligands related to etorphine. |
University of Washington |
| 2153826 |
11 |
Conjugate addition ligands of opioid antagonists. Methacrylate esters and ethers of 6 alpha- and 6 beta-naltrexol. |
University of Washington |
| 10743951 |
9 |
Synthesis of enantiomerically pure (+)- and (-)-18-methoxycoronaridine hydrochloride and their preliminary assessment as anti-addictive agents. |
Albany Molecular Research |
| | 12 |
Synthesis and opioid binding properties of 2-chloroacrylamido derivatives of 7,8-dihydromorphinans |
TBA |
| | 5 |
Suppression of morphine and cocaine self-administration in rats by a mixed mu antagonist-kappa agonist (N-CBM-TAMO) and a long-acting selective D1 antagonist (AS-300) |
TBA |
| | 13 |
N-Methyl and N-cyclopropylmethyl-14α,14′β-[dithiobis[(2-oxo-2,1-ethanediyl)imino]]bis(7,8-dihydro-5β-methyl-morphinone) MET-TAMO and N-CPM-MET-TAMO: Synthesis and opioid binding properties |
TBA |
| 8642554 |
42 |
Asymmetric syntheses, opioid receptor affinities, and antinociceptive effects of 8-amino-5,9-methanobenzocyclooctenes, a new class of structural analogues of the morphine alkaloids. |
Institute |
| 7693944 |
51 |
14 beta-[(p-nitrocinnamoyl)amino]morphinones, 14 beta-[(p-nitrocinnamoyl)amino]-7,8-dihydromorphinones, and their codeinone analogues: synthesis and receptor activity. |
Institute |
| 1315868 |
44 |
Phenylmorphans and analogues: opioid receptor subtype selectivity and effect of conformation on activity. |
Harvard Medical School |
| 25996453 |
4 |
Synthesis of novel 3-aryl-1-oxa-2,8-diazaspiro[4.5]dec-2-ene derivatives and their biological evaluation against protein tyrosine phosphatase 1B. |
Jiangnan University |
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